| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
|
Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
|
20,514 entries
|
There is 0 pattern entry.
|
Closed spina bifida
|
Orphanet_645202 |
|
|
Occult spina bifida
|
Orphanet_645202 |
|
|
Hereditary cranium bifidum
|
Orphanet_60015 |
|
|
Congenital atrioventricular block
|
Orphanet_60041 |
|
|
Congenital heart block
|
Orphanet_60041 |
|
|
Hereditary inclusion body myopathy type 2
|
Orphanet_602 |
|
|
Sporadic inclusion body myositis
|
Orphanet_611 |
|
|
CPP in boy
|
Orphanet_649929 |
|
|
Dysostosis with brachydactyly
|
Orphanet_69028 |
|
|
Preaxial digit brachydactyly-webbed fingers
|
Orphanet_633211 |
|
|
Paraneoplastic isolated brainstem encephalitis
|
Orphanet_624190 |
|
|
Non-syndromic congenital bronchial atresia
|
Orphanet_649010 |
|
|
Isolated left bronchial isomerism
|
Orphanet_649029 |
|
|
Non-syndromic bridging bronchus
|
Orphanet_648992 |
|
|
Pudendal neuralgia by pudendal nerve entrapment
|
Orphanet_60039 |
|
